EP3455218A4 - C3-carbon linked glutarimide degronimers for target protein degradation - Google Patents
C3-carbon linked glutarimide degronimers for target protein degradation Download PDFInfo
- Publication number
- EP3455218A4 EP3455218A4 EP17796809.6A EP17796809A EP3455218A4 EP 3455218 A4 EP3455218 A4 EP 3455218A4 EP 17796809 A EP17796809 A EP 17796809A EP 3455218 A4 EP3455218 A4 EP 3455218A4
- Authority
- EP
- European Patent Office
- Prior art keywords
- target protein
- protein degradation
- carbon linked
- degronimers
- glutarimide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229910052799 carbon Inorganic materials 0.000 title 1
- KNCYXPMJDCCGSJ-UHFFFAOYSA-N piperidine-2,6-dione Chemical compound O=C1CCCC(=O)N1 KNCYXPMJDCCGSJ-UHFFFAOYSA-N 0.000 title 1
- 230000017854 proteolysis Effects 0.000 title 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
- A61K47/545—Heterocyclic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/45—Non condensed piperidines, e.g. piperocaine having oxo groups directly attached to the heterocyclic ring, e.g. cycloheximide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/451—Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
- C07D211/86—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
- C07D211/86—Oxygen atoms
- C07D211/88—Oxygen atoms attached in positions 2 and 6, e.g. glutarimide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
- C07D211/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/22—Bridged ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D495/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
- C07K14/72—Receptors; Cell surface antigens; Cell surface determinants for hormones
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201662334362P | 2016-05-10 | 2016-05-10 | |
PCT/US2017/032041 WO2017197046A1 (en) | 2016-05-10 | 2017-05-10 | C3-carbon linked glutarimide degronimers for target protein degradation |
Publications (2)
Publication Number | Publication Date |
---|---|
EP3455218A1 EP3455218A1 (en) | 2019-03-20 |
EP3455218A4 true EP3455218A4 (en) | 2019-12-18 |
Family
ID=60268035
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP17796809.6A Pending EP3455218A4 (en) | 2016-05-10 | 2017-05-10 | C3-carbon linked glutarimide degronimers for target protein degradation |
Country Status (4)
Country | Link |
---|---|
US (2) | US10849982B2 (en) |
EP (1) | EP3455218A4 (en) |
CN (1) | CN109641874A (en) |
WO (1) | WO2017197046A1 (en) |
Families Citing this family (118)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015117087A1 (en) | 2014-01-31 | 2015-08-06 | Dana-Farber Cancer Institute, Inc. | Uses of diazepane derivatives |
JP2017504653A (en) | 2014-01-31 | 2017-02-09 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | Diaminopyrimidine benzenesulfone derivatives and uses thereof |
US9694084B2 (en) | 2014-12-23 | 2017-07-04 | Dana-Farber Cancer Institute, Inc. | Methods to induce targeted protein degradation through bifunctional molecules |
JP6815318B2 (en) | 2014-12-23 | 2021-01-20 | ダナ−ファーバー キャンサー インスティテュート,インコーポレイテッド | How to Induce Targeted Proteolysis by Bifunctional Molecules |
WO2017007612A1 (en) | 2015-07-07 | 2017-01-12 | Dana-Farber Cancer Institute, Inc. | Methods to induce targeted protein degradation through bifunctional molecules |
RU2750164C2 (en) | 2015-09-11 | 2021-06-22 | Дана-Фарбер Кэнсер Инститьют, Инк. | Cyanothienotriazolodiazepines and methods for their use |
UA123946C2 (en) | 2015-09-11 | 2021-06-30 | Дана-Фарбер Кенсер Інстітьют, Інк. | Acetamide thienotriazolodiazepines and uses thereof |
US10913752B2 (en) | 2015-11-25 | 2021-02-09 | Dana-Farber Cancer Institute, Inc. | Bivalent bromodomain inhibitors and uses thereof |
US10532103B2 (en) * | 2016-04-22 | 2020-01-14 | Dana-Farber Cancer Institute, Inc. | Degradation of cyclin-dependent kinase 9 (CDK9) by conjugation of CDK9 inhibitors with E3 ligase ligand and methods of use |
AU2017254713C1 (en) | 2016-04-22 | 2021-04-29 | Dana-Farber Cancer Institute, Inc. | Bifunctional molecules for degradation of EGFR and methods of use |
CN109562107A (en) | 2016-05-10 | 2019-04-02 | C4医药公司 | Heterocycle degron body for target protein degradation |
CN109562113A (en) | 2016-05-10 | 2019-04-02 | C4医药公司 | Loop coil degron body for target protein degradation |
CA3034326A1 (en) | 2016-08-19 | 2018-02-22 | Beigene, Ltd. | Use of a combination comprising a btk inhibitor for treating cancers |
WO2018064589A1 (en) | 2016-09-29 | 2018-04-05 | Dana-Farber Cancer Institute, Inc. | Targeted protein degradation using a mutant e3 ubiquitin ligase |
MX2019004278A (en) | 2016-10-11 | 2019-08-05 | Arvinas Inc | Compounds and methods for the targeted degradation of androgen receptor. |
WO2018165520A1 (en) | 2017-03-10 | 2018-09-13 | Vps-3, Inc. | Metalloenzyme inhibitor compounds |
EP3641762A4 (en) | 2017-06-20 | 2021-03-10 | C4 Therapeutics, Inc. | N/o-linked degrons and degronimers for protein degradation |
AU2018290532A1 (en) | 2017-06-26 | 2019-11-21 | Beigene, Ltd. | Immunotherapy for hepatocellular carcinoma |
CN111278816B (en) | 2017-09-04 | 2024-03-15 | C4医药公司 | Dihydro quinolinones |
CN118108706A (en) | 2017-09-04 | 2024-05-31 | C4医药公司 | Glutarimide |
WO2019060693A1 (en) * | 2017-09-22 | 2019-03-28 | Kymera Therapeutics, Inc. | Crbn ligands and uses thereof |
EP3684365A4 (en) | 2017-09-22 | 2021-09-08 | Kymera Therapeutics, Inc. | Protein degraders and uses thereof |
EP3710002A4 (en) | 2017-11-16 | 2021-07-07 | C4 Therapeutics, Inc. | Degraders and degrons for targeted protein degradation |
CN111801334B (en) | 2017-11-29 | 2023-06-09 | 百济神州瑞士有限责任公司 | Treatment of indolent or invasive B-cell lymphomas using combinations comprising BTK inhibitors |
IL315310A (en) | 2017-12-26 | 2024-10-01 | Kymera Therapeutics Inc | Irak degraders and uses thereof |
EP3737666A4 (en) | 2018-01-12 | 2022-01-05 | Kymera Therapeutics, Inc. | Protein degraders and uses thereof |
US11512080B2 (en) | 2018-01-12 | 2022-11-29 | Kymera Therapeutics, Inc. | CRBN ligands and uses thereof |
WO2019152440A1 (en) | 2018-01-30 | 2019-08-08 | Foghorn Therapeutics Inc. | Methods and compounds for treating disorders |
TW201945357A (en) * | 2018-02-05 | 2019-12-01 | 瑞士商赫孚孟拉羅股份公司 | Compounds |
US11542251B2 (en) | 2018-02-14 | 2023-01-03 | Dana-Farber Cancer Institute, Inc. | IRAK degraders and uses thereof |
CR20240101A (en) | 2018-03-08 | 2024-05-24 | Incyte Corp | AMINOPYRAZINE DIOL COMPOUNDS AS PI3K-y INHIBITORS |
JP2021519337A (en) | 2018-03-26 | 2021-08-10 | シー4 セラピューティクス, インコーポレイテッド | Cereblon binder for the degradation of Ikaras |
WO2019204354A1 (en) | 2018-04-16 | 2019-10-24 | C4 Therapeutics, Inc. | Spirocyclic compounds |
EP3578561A1 (en) | 2018-06-04 | 2019-12-11 | F. Hoffmann-La Roche AG | Spiro compounds |
US11046658B2 (en) | 2018-07-02 | 2021-06-29 | Incyte Corporation | Aminopyrazine derivatives as PI3K-γ inhibitors |
EP3817748A4 (en) | 2018-07-06 | 2022-08-24 | Kymera Therapeutics, Inc. | Tricyclic crbn ligands and uses thereof |
US11639354B2 (en) | 2018-07-31 | 2023-05-02 | Fimecs, Inc. | Heterocyclic compound |
IL280984B1 (en) | 2018-08-22 | 2024-10-01 | Cullgen Shanghai Inc | Tropomyosin receptor kinase (trk) degradation compounds and methods of use |
US11969472B2 (en) | 2018-08-22 | 2024-04-30 | Cullgen (Shanghai), Inc. | Tropomyosin receptor kinase (TRK) degradation compounds and methods of use |
EP3846800A4 (en) | 2018-09-04 | 2022-08-24 | C4 Therapeutics, Inc. | Compounds for the degradation of brd9 or mth1 |
WO2020048546A1 (en) * | 2018-09-07 | 2020-03-12 | 南京明德新药研发有限公司 | Tricyclic substituted piperidine dione compound |
US12098137B2 (en) | 2018-09-07 | 2024-09-24 | Sumitomo Chemical Company, Limited | Method for manufacturing cyclopropane compound |
JP7323603B2 (en) * | 2018-09-07 | 2023-08-08 | メッドシャイン ディスカバリー インコーポレイテッド | Tricyclic Fused Furan-Substituted Piperidinedione Compounds |
EP3866801A4 (en) * | 2018-10-16 | 2022-11-09 | Dana-Farber Cancer Institute, Inc. | Degraders of wild-type and mutant forms of lrrk2 |
CN112969696B (en) * | 2018-11-02 | 2024-06-11 | 达纳-法伯癌症研究公司 | Development and use of acetylated writer inhibitors |
US10844039B2 (en) | 2018-11-13 | 2020-11-24 | Biotheryx, Inc. | Substituted isoindolinones |
MX2021006154A (en) | 2018-11-30 | 2021-08-24 | Kymera Therapeutics Inc | Irak degraders and uses thereof. |
MX2021007475A (en) | 2018-12-19 | 2021-08-05 | Celgene Corp | Substituted 3-((3-aminophenyl)amino)piperidine-2,6-dione compounds, compositions thereof, and methods of treatment therewith. |
TWI820276B (en) | 2018-12-19 | 2023-11-01 | 美商西建公司 | Substituted 3-((3-aminophenyl)amino)piperidine-2,6-dione compounds, compositions thereof, and methods of treatment therewith |
WO2020132561A1 (en) | 2018-12-20 | 2020-06-25 | C4 Therapeutics, Inc. | Targeted protein degradation |
US20230066136A1 (en) | 2019-01-29 | 2023-03-02 | Foghorn Therapeutics Inc. | Compounds and uses thereof |
WO2020162725A1 (en) * | 2019-02-07 | 2020-08-13 | 한국화학연구원 | Target protein eed degradation-inducing degraducer, preparation method thereof, and pharmaceutical composition for preventing or treating diseases related to eed, ezh2, or prc2, comprising same as active ingredient |
CN113557235A (en) | 2019-03-06 | 2021-10-26 | C4医药公司 | Heterocyclic compounds for use in medical therapy |
WO2020191369A1 (en) | 2019-03-21 | 2020-09-24 | Codiak Biosciences, Inc. | Process for preparing extracellular vesicles |
CN113747925B (en) | 2019-03-21 | 2024-10-15 | 隆萨销售股份公司 | Extracellular vesicle conjugates and uses thereof |
CA3130706A1 (en) | 2019-04-04 | 2020-10-08 | Dana-Farber Cancer Institute, Inc. | Cdk2/5 degraders and uses thereof |
TW202106676A (en) | 2019-04-05 | 2021-02-16 | 美商凱麥拉醫療公司 | Stat degraders and uses thereof |
CN114007652A (en) * | 2019-06-18 | 2022-02-01 | 达纳-法伯癌症研究公司 | Small molecule targeted bromo/acetyl protein and application thereof |
WO2020264499A1 (en) | 2019-06-28 | 2020-12-30 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
WO2021030358A1 (en) | 2019-08-12 | 2021-02-18 | Regeneron Pharmaceuticals, Inc. | Macrophage stimulating 1 receptor (mst1r) variants and uses thereof |
CA3150653A1 (en) * | 2019-09-12 | 2021-03-18 | Yunfu Luo | Fused cyclic compound capable of degrading protein and use thereof |
WO2021127283A2 (en) | 2019-12-17 | 2021-06-24 | Kymera Therapeutics, Inc. | Irak degraders and uses thereof |
KR20220145325A (en) | 2019-12-17 | 2022-10-28 | 카이메라 쎄라퓨틱스 인코포레이티드 | IRAK disintegrants and uses thereof |
US11883393B2 (en) | 2019-12-19 | 2024-01-30 | Arvinas Operations, Inc. | Compounds and methods for the targeted degradation of androgen receptor |
EP4076450A4 (en) | 2019-12-20 | 2024-01-10 | C4 Therapeutics, Inc. | Isoindolinone and indazole compounds for the degradation of egfr |
EP4077319A1 (en) * | 2019-12-20 | 2022-10-26 | Calico Life Sciences LLC | Protein tyrosine phosphatase degraders and methods of use thereof |
IL294150A (en) | 2019-12-23 | 2022-08-01 | Kymera Therapeutics Inc | Smarca degraders and uses thereof |
EP4096651A4 (en) | 2020-01-29 | 2024-01-24 | Foghorn Therapeutics Inc. | Compounds and uses thereof |
CN115697989A (en) * | 2020-02-26 | 2023-02-03 | 上海睿跃生物科技有限公司 | Tropomyosin Receptor Kinase (TRK) degrading compounds and methods of use |
CN115279370A (en) | 2020-03-05 | 2022-11-01 | C4医药公司 | Compounds for targeted degradation of BRD9 |
EP4122925A4 (en) * | 2020-03-17 | 2024-04-17 | Medshine Discovery Inc. | Proteolysis regulator and method for using same |
MX2022011602A (en) | 2020-03-19 | 2023-01-04 | Kymera Therapeutics Inc | Mdm2 degraders and uses thereof. |
TW202208345A (en) | 2020-05-09 | 2022-03-01 | 美商亞文納營運公司 | Methods of manufacturing a bifunctional compound, ultrapure forms of the bifunctional compound, and dosage forms comprising the same |
CN111606969B (en) * | 2020-05-13 | 2023-02-03 | 四川大学 | PARP1 protein degradation agent and application thereof in tumor resistance |
WO2021237100A1 (en) | 2020-05-21 | 2021-11-25 | Codiak Biosciences, Inc. | Methods of targeting extracellular vesicles to lung |
TW202210483A (en) | 2020-06-03 | 2022-03-16 | 美商凱麥拉醫療公司 | Crystalline forms of irak degraders |
JP2023531495A (en) * | 2020-06-24 | 2023-07-24 | セルジーン コーポレーション | Cereblon binding compounds, compositions thereof and methods of treatment therewith |
BR112022025933A2 (en) * | 2020-06-24 | 2023-01-10 | Celgene Corp | CEREBLON-BINDING COMPOUNDS, COMPOSITIONS THEREOF, AND TREATMENT METHODS THEREOF |
AR122725A1 (en) | 2020-06-24 | 2022-09-28 | Celgene Corp | CEREBLON JUNCTION COMPOUNDS, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREOF |
US11839659B2 (en) | 2020-07-02 | 2023-12-12 | Northwestern University | Proteolysis-targeting chimeric molecules (PROTACs) that induce degradation of indoleamine 2,3-dioxygenase (IDO) protein |
US11787800B2 (en) | 2020-07-29 | 2023-10-17 | Foghorn Therapeutics Inc. | BRD9 degraders and uses thereof |
WO2022051616A1 (en) * | 2020-09-03 | 2022-03-10 | Board Of Regents Of The University Of Nebraska | Cdk targeted heterobifunctional small molecule proteolysis targeting chimeras |
WO2022066928A2 (en) | 2020-09-23 | 2022-03-31 | Codiak Biosciences, Inc. | Process for preparing extracellular vesicles |
WO2022120355A1 (en) | 2020-12-02 | 2022-06-09 | Ikena Oncology, Inc. | Tead degraders and uses thereof |
WO2022146151A1 (en) * | 2020-12-30 | 2022-07-07 | Captor Therapeutics S.A. | Novel compounds which bind to cereblon, and methods of use thereof |
CN116847848A (en) * | 2021-02-10 | 2023-10-03 | 百济神州有限公司 | EGFR degrading agents and methods of use |
TW202302567A (en) | 2021-03-29 | 2023-01-16 | 大陸商江蘇恆瑞醫藥股份有限公司 | Tetrahydronaphthalene compounds, preparation method and medical use thereof |
US11981678B2 (en) | 2021-04-29 | 2024-05-14 | Northwestern University | Substituted [1,2,4]triazolo[4,3-c]pyrimidin-5-amines and proteolysis-targeting chimeric derivatives thereof (PROTACs) that induce degradation of embryonic ectoderm development (EED) protein |
US12042543B2 (en) | 2021-04-30 | 2024-07-23 | Northwestern University | Substituted 3-amino-5-phenylbenzamide compounds as covalent inhibitors of enhancer zeste homolog 2 (EZH2) and proteolysis-targeting chimeric derivatives thereof (PROTACs) that induce degradation of EZH2 |
WO2022235945A1 (en) | 2021-05-05 | 2022-11-10 | Biogen Ma Inc. | Compounds for targeting degradation of bruton's tyrosine kinase |
MX2023013173A (en) | 2021-05-07 | 2023-11-30 | Kymera Therapeutics Inc | Cdk2 degraders and uses thereof. |
IL308748A (en) * | 2021-06-08 | 2024-01-01 | C4 Therapeutics Inc | Therapeutics for the degradation of mutant braf |
WO2022262782A1 (en) * | 2021-06-17 | 2022-12-22 | 南京明德新药研发有限公司 | Glutarimide-substituted isoxazole fused ring compound, and application thereof |
AU2022300033A1 (en) * | 2021-06-21 | 2024-01-18 | Beigene Switzerland Gmbh | (r) -glutarimide crbn ligands and methods of use |
CA3223322A1 (en) * | 2021-06-21 | 2022-12-29 | Gesine Kerstin Veits | Degrader compounds and uses thereof |
WO2023283130A1 (en) | 2021-07-04 | 2023-01-12 | Newave Pharmaceutical Inc. | Isoquinoline derivatives as mutant egfr modulators and uses thereof |
WO2023283263A1 (en) | 2021-07-06 | 2023-01-12 | Foghorn Therapeutics Inc. | Citrate salt, pharmaceutical compositions, and methods of making and using the same |
KR20240035526A (en) | 2021-07-07 | 2024-03-15 | 바이오젠 엠에이 인코포레이티드 | Compounds that target degradation of the IRAK4 protein |
JP2024525580A (en) | 2021-07-07 | 2024-07-12 | バイオジェン・エムエイ・インコーポレイテッド | Compounds for targeting the degradation of IRAK4 protein |
JP2024531273A (en) | 2021-08-18 | 2024-08-29 | ニューリックス セラピューティクス,インコーポレイテッド | Bifunctional degraders of interleukin-1 receptor associated kinase and their therapeutic uses |
WO2023055952A1 (en) * | 2021-09-29 | 2023-04-06 | C4 Therapeutics, Inc. | Neurotrophic tyrosine receptor kinase (ntrk) degrading compounds |
KR20240111312A (en) | 2021-10-25 | 2024-07-16 | 카이메라 쎄라퓨틱스 인코포레이티드 | TYK2 degrader and its uses |
TW202333695A (en) * | 2022-01-27 | 2023-09-01 | 大陸商四川海思科製藥有限公司 | Nitrogen-containing heteroaromatic ring compound as well as composition and pharmaceutical use thereof |
WO2023143249A1 (en) * | 2022-01-28 | 2023-08-03 | 上海齐鲁制药研究中心有限公司 | Protein degradation compound targeting malt1 |
KR20240144266A (en) | 2022-01-31 | 2024-10-02 | 카이메라 쎄라퓨틱스 인코포레이티드 | IRAK decomposer and its uses |
WO2023205701A1 (en) | 2022-04-20 | 2023-10-26 | Kumquat Biosciences Inc. | Macrocyclic heterocycles and uses thereof |
CN114853751B (en) * | 2022-05-13 | 2024-01-16 | 郑州大学第一附属医院 | Group of phenothiazine derivatives and application thereof |
CN114957101B (en) * | 2022-05-24 | 2023-11-28 | 山东第一医科大学(山东省医学科学院) | Synthesis method of 3-aryl substituted dipiperidone and nilaparil |
WO2023250029A1 (en) * | 2022-06-22 | 2023-12-28 | Nikang Therapeutics, Inc. | Bifunctional compounds containing substituted pyrimidine derivatives for degrading cyclin-dependent kinase 2 via ubiquitin proteasome pathway |
WO2024006776A1 (en) | 2022-06-27 | 2024-01-04 | Relay Therapeutics, Inc. | Estrogen receptor alpha degraders and medical use thereof |
WO2024006781A1 (en) | 2022-06-27 | 2024-01-04 | Relay Therapeutics, Inc. | Estrogen receptor alpha degraders and use thereof |
WO2024050016A1 (en) | 2022-08-31 | 2024-03-07 | Oerth Bio Llc | Compositions and methods for targeted inhibition and degradation of proteins in an insect cell |
WO2024064358A1 (en) | 2022-09-23 | 2024-03-28 | Ifm Due, Inc. | Compounds and compositions for treating conditions associated with sting activity |
WO2024073507A1 (en) | 2022-09-28 | 2024-04-04 | Theseus Pharmaceuticals, Inc. | Macrocyclic compounds and uses thereof |
WO2024102810A1 (en) * | 2022-11-08 | 2024-05-16 | Montelino Therapeutics, Inc. | Bi-functional compounds and methods for targeted ubiquitination of androgen receptor |
WO2024123195A1 (en) * | 2022-12-06 | 2024-06-13 | Captor Therapeutics S.A. | Targeted protein degradation using prodrugs of bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein |
WO2024121256A1 (en) * | 2022-12-06 | 2024-06-13 | Captor Therapeutics S.A. | Targeted protein degradation using bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein |
WO2024205320A2 (en) * | 2023-03-29 | 2024-10-03 | 주식회사 아이비스바이오 | Small molecule compound exhibiting cereblon-binding activity, and use thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007031791A1 (en) * | 2005-09-16 | 2007-03-22 | Arrow Therapeutics Limited | Biphenyl derivatives and their use in treating hepatitis c |
WO2013089278A1 (en) * | 2011-12-14 | 2013-06-20 | Taiho Pharmaceutical Co., Ltd. | Recombinant prpk-tprkb and uses thereof |
WO2014023081A1 (en) * | 2012-08-07 | 2014-02-13 | 中国科学院上海生命科学研究院 | Artemisinin derivatives, preparation process and use thereof |
US20160058872A1 (en) * | 2014-04-14 | 2016-03-03 | Arvinas, Inc. | Imide-based modulators of proteolysis and associated methods of use |
Family Cites Families (397)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4418068A (en) | 1981-04-03 | 1983-11-29 | Eli Lilly And Company | Antiestrogenic and antiandrugenic benzothiophenes |
TW366342B (en) | 1992-07-28 | 1999-08-11 | Lilly Co Eli | The use of 2-phenyl-3-aroylbenzothiophenes in inhibiting bone loss |
US5565215A (en) | 1993-07-23 | 1996-10-15 | Massachusettes Institute Of Technology | Biodegradable injectable particles for imaging |
US5478847A (en) | 1994-03-02 | 1995-12-26 | Eli Lilly And Company | Methods of use for inhibiting bone loss and lowering serum cholesterol |
GB9412273D0 (en) | 1994-06-18 | 1994-08-10 | Univ Nottingham | Administration means |
US6007845A (en) | 1994-07-22 | 1999-12-28 | Massachusetts Institute Of Technology | Nanoparticles and microparticles of non-linear hydrophilic-hydrophobic multiblock copolymers |
US6413539B1 (en) | 1996-10-31 | 2002-07-02 | Poly-Med, Inc. | Hydrogel-forming, self-solvating absorbable polyester copolymers, and methods for use thereof |
CA2233888A1 (en) | 1995-10-06 | 1997-04-10 | Ligand Pharmaceuticals Incorporated | Dimer-selective rxr modulators and methods for their use |
TW397821B (en) | 1996-04-19 | 2000-07-11 | American Home Produits Corp | 3-[4-(2-phenyl-indole-1-ylmethyl)-phenyl]-acrylamides and 2-phenyl-1-[4-(amino-1-yl-alk-1-ynyl)-benzyl]-1H-indol-5-ol as well as pharmaceutical compositions of estrogenic agents thereof |
US5780497A (en) | 1996-04-19 | 1998-07-14 | American Home Products Corporation | 2-phenyl-1- 4-(amino-1-yl-alk-1-ynyl)-benzyl!-1H-indol-5-ols as estrogenic agents |
US5998402A (en) | 1996-04-19 | 1999-12-07 | American Home Products Corporation | 2-phenyl-1-[4-(2-aminoethoxy)-benzyl]-indoles as estrogenic agents |
US5880137A (en) | 1996-04-19 | 1999-03-09 | American Home Products Corporation | 2-phenyl-1- 4-(amino-1-yl-alk-1-ynyl)-benzyl!-1H-indol-5-ols as estrogenic agents |
US5635517B1 (en) | 1996-07-24 | 1999-06-29 | Celgene Corp | Method of reducing TNFalpha levels with amino substituted 2-(2,6-dioxopiperidin-3-YL)-1-oxo-and 1,3-dioxoisoindolines |
WO1998011111A1 (en) | 1996-09-13 | 1998-03-19 | Yoshitomi Pharmaceutical Industries, Ltd. | Thienotriazolodiazepine compounds and medicinal uses thereof |
US6005102A (en) | 1997-10-15 | 1999-12-21 | American Home Products Corporation | Aryloxy-alkyl-dialkylamines |
US6326392B1 (en) | 1997-11-06 | 2001-12-04 | American Home Products Corporation | Anti-estrogen plus progestin containing oral contraceptives |
UA68365C2 (en) | 1997-11-06 | 2004-08-16 | Wyeth Corp | Peroral contraception by combination of anti-estrogen and progestin |
JP4204657B2 (en) | 1997-12-05 | 2009-01-07 | 有限会社ケムフィズ | Diabetes prevention and treatment |
FR2776657B1 (en) | 1998-03-31 | 2000-05-26 | Cird Galderma | BICYCLIC-AROMATIC COMPOUNDS AND THEIR USE IN HUMAN OR VETERINARY MEDICINE AND IN COSMETOLOGY |
US6479535B1 (en) | 1998-05-15 | 2002-11-12 | Wyeth | 2-phenyl-1-[4-(2-aminoethoxy)-benzyl]-indole and estrogen formulations |
US6583170B1 (en) | 1998-05-15 | 2003-06-24 | Wyeth | 2-Phenyl-1-[4-(amino-1-yl-alk-1-ynyl)-benzyl]-1H-indol-5-ol and estrogen formulations |
US6306663B1 (en) | 1999-02-12 | 2001-10-23 | Proteinex, Inc. | Controlling protein levels in eucaryotic organisms |
US6287588B1 (en) | 1999-04-29 | 2001-09-11 | Macromed, Inc. | Agent delivering system comprised of microparticle and biodegradable gel with an improved releasing profile and methods of use thereof |
CO5271709A1 (en) | 2000-01-12 | 2003-04-30 | Pfizer Prod Inc | COMPOSITIONS AND PROCEDURES FOR THE AND TREATMENT OF AFFECTIONS RESPONDING TO STROGENS |
CO5271697A1 (en) | 2000-01-12 | 2003-04-30 | Pfizer Prod Inc | COMPOSITIONS AND PROCEDURES FOR THE TREATMENT OF AFFECTIONS THAT RESPOND TO AN INCREASE OF TESTOSTERONE |
CO5271696A1 (en) | 2000-01-12 | 2003-04-30 | Pfizer Prod Inc | PROCEDURE TO REDUCE MORBILITY AND RISK OF MORTALITY |
CO5251465A1 (en) | 2000-01-26 | 2003-02-28 | Pfizer Prod Inc | COMPOSITIONS AND PROCEDURES TO TREAT OSTEOPOROSIS AND REDUCE CHOLESTEROL |
US20020013327A1 (en) | 2000-04-18 | 2002-01-31 | Lee Andrew G. | Compositions and methods for treating female sexual dysfunction |
US6589549B2 (en) | 2000-04-27 | 2003-07-08 | Macromed, Incorporated | Bioactive agent delivering system comprised of microparticles within a biodegradable to improve release profiles |
MY164523A (en) | 2000-05-23 | 2017-12-29 | Univ Degli Studi Cagliari | Methods and compositions for treating hepatitis c virus |
US6495164B1 (en) | 2000-05-25 | 2002-12-17 | Alkermes Controlled Therapeutics, Inc. I | Preparation of injectable suspensions having improved injectability |
EP1736478B1 (en) | 2000-05-26 | 2015-07-22 | IDENIX Pharmaceuticals, Inc. | Methods and compositions for treating flaviviruses and pestiviruses |
WO2002003986A2 (en) | 2000-07-06 | 2002-01-17 | Wyeth | Use of substituted indole compounds for treating breast disorders |
EP1311293A2 (en) | 2000-07-06 | 2003-05-21 | Wyeth | Combinations of ssri and estrogenic agents |
US6509332B2 (en) | 2000-07-06 | 2003-01-21 | Wyeth | Methods of treating excessive intraocular pressure |
AR030064A1 (en) | 2000-07-06 | 2003-08-13 | Wyeth Corp | METHODS TO INHIBIT THE UTEROTROPHIC EFFECTS OF ESTROGEN AGENTS |
MXPA02012896A (en) | 2000-07-06 | 2003-10-24 | Wyeth Corp | Combinations of statins, estrogenic agents and optionally estrogens. |
AU2001271781A1 (en) | 2000-07-06 | 2002-01-21 | Wyeth | Use of substituted indole compounds for treating sphincter incontinence |
WO2002003992A2 (en) | 2000-07-06 | 2002-01-17 | Wyeth | Use of substituted indole compounds for treating prosthesis-related bone degeneration |
WO2002003988A2 (en) | 2000-07-06 | 2002-01-17 | Wyeth | Use of substituted indole compounds for treating neuropeptide y-related conditions |
US20020022617A1 (en) | 2000-07-06 | 2002-02-21 | American Home Products Corporation | Methods for increasing nitric oxide synthase activity |
AU2001273125A1 (en) | 2000-07-06 | 2002-01-21 | American Home Products Corporation | Combinations of bisphosphonates, estrogenic agents and optionally estrogens |
EP1177787A3 (en) | 2000-07-28 | 2003-09-10 | Pfizer Products Inc. | Use of an estrogen agonist/antagonist for treating cataracts |
AU2001283139A1 (en) | 2000-08-11 | 2002-02-25 | Wyeth | Method of treating estrogen receptor positive carcinoma |
PE20020354A1 (en) | 2000-09-01 | 2002-06-12 | Novartis Ag | HYDROXAMATE COMPOUNDS AS HISTONE-DESACETILASE (HDA) INHIBITORS |
US7208157B2 (en) | 2000-09-08 | 2007-04-24 | California Institute Of Technology | Proteolysis targeting chimeric pharmaceutical |
EP1322750A4 (en) | 2000-09-08 | 2004-09-29 | California Inst Of Techn | Proteolysis targeting chimeric pharmaceutical |
EP1192945A3 (en) | 2000-09-21 | 2004-03-03 | Pfizer Products Inc. | Use of an estrogen agonist/antagonist for treating osteoarthritis |
IL145838A (en) | 2000-10-16 | 2008-11-03 | Pfizer Prod Inc | Use of an estrogen agonist/antagonist for the manufacture of a medicament for treating vaginitis |
EP1353701B1 (en) | 2000-10-31 | 2011-12-21 | PR Pharmaceuticals, Inc. | Methods for producing compositions for enhanced delivery of bioactive molecules |
US20030045552A1 (en) | 2000-12-27 | 2003-03-06 | Robarge Michael J. | Isoindole-imide compounds, compositions, and uses thereof |
US8481712B2 (en) | 2001-01-22 | 2013-07-09 | Merck Sharp & Dohme Corp. | Nucleoside derivatives as inhibitors of RNA-dependent RNA viral polymerase |
AU781168B2 (en) | 2001-01-26 | 2005-05-12 | Pfizer Products Inc. | Method of treating certain cancers using an estrogen agonist/antagonist |
AU2002259130A1 (en) | 2001-05-03 | 2002-11-18 | Eli Lilly And Company | Agents for treatment of hcv and methods of use |
WO2003070750A2 (en) | 2002-02-20 | 2003-08-28 | Sirna Therapeutics, Inc | Rna interference mediated inhibition of hepatitis c virus |
GB0122318D0 (en) | 2001-09-14 | 2001-11-07 | Novartis Ag | Organic compounds |
WO2003026589A2 (en) | 2001-09-28 | 2003-04-03 | Idenix (Cayman) Limited | Methods and compositions for treating hepatitis c virus using 4'-modified nucleosides |
US7935812B2 (en) | 2002-02-20 | 2011-05-03 | Merck Sharp & Dohme Corp. | RNA interference mediated inhibition of hepatitis C virus (HCV) expression using short interfering nucleic acid (siNA) |
US7608600B2 (en) | 2002-06-28 | 2009-10-27 | Idenix Pharmaceuticals, Inc. | Modified 2′ and 3′-nucleoside prodrugs for treating Flaviviridae infections |
US7456155B2 (en) | 2002-06-28 | 2008-11-25 | Idenix Pharmaceuticals, Inc. | 2′-C-methyl-3′-O-L-valine ester ribofuranosyl cytidine for treatment of flaviviridae infections |
CN101172993A (en) | 2002-06-28 | 2008-05-07 | 埃迪尼克斯(开曼)有限公司 | 2'-c-methyl-3'-o-l-valine ester ribofuranosyl cytidine for treatment of flaviviridae infections |
GB0215293D0 (en) | 2002-07-03 | 2002-08-14 | Rega Foundation | Viral inhibitors |
US20060069067A1 (en) | 2002-07-30 | 2006-03-30 | Bhatnagar Ajay S | Combination of an aromatase inhibitor with a bisphosphonate |
DK1576138T3 (en) | 2002-11-15 | 2017-05-01 | Idenix Pharmaceuticals Llc | 2'-METHYL NUCLEOSIDES IN COMBINATION WITH INTERFERON AND FLAVIVIRIDAE MUTATION |
CA2506415A1 (en) | 2002-11-19 | 2004-06-03 | Achillion Pharmaceuticals, Inc. | Substituted aryl thioureas and releated compounds; inhibitors of viral replication |
US20060234982A1 (en) | 2003-01-14 | 2006-10-19 | Dahl Terrence C | Compositions and methods for combination antiviral therapy |
US7871607B2 (en) | 2003-03-05 | 2011-01-18 | Halozyme, Inc. | Soluble glycosaminoglycanases and methods of preparing and using soluble glycosaminoglycanases |
CA2522067C (en) | 2003-04-09 | 2010-07-06 | Canadian Blood Services | Detection, characterization and treatment of viral infection and methods thereof |
DK1628685T3 (en) | 2003-04-25 | 2011-03-21 | Gilead Sciences Inc | Antiviral phosphonate analogues |
CA2527657C (en) | 2003-05-30 | 2011-06-14 | Pharmasset, Inc. | Modified fluorinated nucleoside analogues |
BRPI0412502A (en) | 2003-07-10 | 2006-09-19 | Achillion Pharmaceuticals Inc | substituted arylthiourea derivatives useful as viral replication inhibitors |
US20050009910A1 (en) | 2003-07-10 | 2005-01-13 | Allergan, Inc. | Delivery of an active drug to the posterior part of the eye via subconjunctival or periocular delivery of a prodrug |
JP2007501185A (en) | 2003-07-25 | 2007-01-25 | イデニクス(ケイマン)リミテツド | Purine nucleoside analogues for treating flavivirus related diseases including hepatitis C |
WO2006089054A1 (en) | 2005-02-16 | 2006-08-24 | Achillion Pharmaceuticals, Inc. | New isothiazoloquinolones and related compounds as anti-infective agents |
CA2543846C (en) | 2003-11-05 | 2011-04-12 | Merck & Co., Inc. | Hcv replicons containing ns5b from genotype 2b |
PL1706403T3 (en) | 2003-12-22 | 2012-07-31 | K U Leuven Res & Development | Imidazo[4,5-c]pyridine compounds and methods of antiviral treatment |
TW200528459A (en) | 2004-01-06 | 2005-09-01 | Achillion Pharmaceuticals Inc | Azabenzofuran substituted thioureas; inhibitors of viral replication |
WO2005070957A1 (en) | 2004-01-09 | 2005-08-04 | Merck & Co., Inc. | Hcv rna-dependent rna polymerase |
JP2007530049A (en) | 2004-03-24 | 2007-11-01 | アキリオン ファーマシューティカルズ,インコーポレーテッド | Quantitative assays for detection of newly synthesized RNA and identification of RNA synthesis inhibitors in cell-free systems |
WO2005097618A2 (en) | 2004-04-01 | 2005-10-20 | Achillion Pharmaceuticals, Inc. | Low dose therapy for treating viral infections |
ES2246694B1 (en) | 2004-04-29 | 2007-05-01 | Instituto Cientifico Y Tecnologico De Navarra, S.A. | PEGILATED NANOPARTICLES. |
US20050244469A1 (en) | 2004-04-30 | 2005-11-03 | Allergan, Inc. | Extended therapeutic effect ocular implant treatments |
WO2005107708A1 (en) | 2004-04-30 | 2005-11-17 | Allergan, Inc. | Biodegradable intravitreal tyrosine kinase inhibitors implants |
US7771742B2 (en) | 2004-04-30 | 2010-08-10 | Allergan, Inc. | Sustained release intraocular implants containing tyrosine kinase inhibitors and related methods |
TW200600492A (en) | 2004-05-18 | 2006-01-01 | Achillion Pharmaceuticals Inc | Substituted aryl acylthioureas and related compounds; inhibitors of viral replication |
EP1758453B1 (en) | 2004-06-15 | 2014-07-16 | Merck Sharp & Dohme Corp. | C-purine nucleoside analogs as inhibitors of rna-dependent rna viral polymerase |
US7842815B2 (en) | 2004-06-17 | 2010-11-30 | Infinity Pharmaceuticals, Inc. | Compounds and methods for inhibiting the interaction of BCL proteins with binding partners |
CN101023094B (en) | 2004-07-21 | 2011-05-18 | 法莫赛特股份有限公司 | Preparation of alkyl-substituted 2-deoxy-2-fluoro-d-ribofuranosyl pyrimidines and purines and their derivatives |
CA2574514A1 (en) | 2004-07-27 | 2006-10-19 | Gilead Sciences, Inc. | Phosphonate analogs of hiv inhibitor compounds |
SG158136A1 (en) | 2004-09-14 | 2010-01-29 | Pharmasset Inc | Preparation of 2`-fluoro-2`- alkyl- substituted or other optionally substituted ribofuranosyl pyrimidines and purines and their derivatives |
MX2007007779A (en) | 2004-12-23 | 2007-08-14 | Novartis Ag | Compositions for hcv treatment. |
US7659399B2 (en) | 2005-01-05 | 2010-02-09 | Achillion Pharmaceuticals, Inc. | 1-thia-2,4a-diaza-cyclopenta[b]napththalene-3,4-diones and related compounds as anti-infective agents |
AU2006206446A1 (en) | 2005-01-21 | 2006-07-27 | Janssen Pharmaceutica N.V. | Novel heterocyclic benzo[c]chromene derivatives useful as modulators of the estrogen receptors |
US7199128B2 (en) | 2005-02-02 | 2007-04-03 | Achillion Pharmaceuticals, Inc. | 8-N-substituted-2H-isothiazolo[5,4-b]quinolizine-3,4-diones and related compounds as antiinfective agents |
US8999289B2 (en) | 2005-03-22 | 2015-04-07 | President And Fellows Of Harvard College | Treatment of protein degradation disorders |
CA2606195C (en) | 2005-05-02 | 2015-03-31 | Merck And Co., Inc. | Hcv ns3 protease inhibitors |
SG159561A1 (en) | 2005-05-09 | 2010-03-30 | Achillion Pharmaceuticals Inc | Thiazole compounds and methods of use |
ES2302402B1 (en) | 2005-06-16 | 2009-05-08 | Proyecto De Biomedicina Cima, S.L. | USE OF A CYTOQUINE OF THE INTERLEUQUINA-6 FAMILY IN THE PREPARATION OF A COMPOSITION FOR ADMINISTRATION COMBINED WITH INTERFERON-ALFA. |
CN101213204B (en) | 2005-06-17 | 2013-06-19 | P.安杰莱蒂分子生物学研究所 | Hepatitis c virus nucleic acid vaccine |
US8232278B2 (en) | 2005-06-24 | 2012-07-31 | Gilead Sciences, Inc. | Pyrido(3,2-D)pyrimidines and pharmaceutical compositions useful for treating hepatitis C |
AR057456A1 (en) | 2005-07-20 | 2007-12-05 | Merck & Co Inc | HCV PROTEASA NS3 INHIBITORS |
JP5143000B2 (en) | 2005-07-27 | 2013-02-13 | アキリオン ファーマシューティカルズ,インコーポレーテッド | 8-methoxy-9H-isothiazolo [5,4-b] quinoline-3,4-dione and related compounds as anti-infective agents |
KR20080036598A (en) | 2005-08-01 | 2008-04-28 | 머크 앤드 캄파니 인코포레이티드 | Macrocyclic peptides as hcv ns3 protease inhibitors |
WO2007021610A2 (en) | 2005-08-09 | 2007-02-22 | Merck & Co., Inc. | Ribonucleoside cyclic acetal derivatives for the treatment of rna-dependent rna viral infection |
GB0518971D0 (en) * | 2005-09-16 | 2005-10-26 | Arrow Therapeutics Ltd | Chemical compounds |
US20070071756A1 (en) | 2005-09-26 | 2007-03-29 | Peyman Gholam A | Delivery of an agent to ameliorate inflammation |
JP2009510075A (en) | 2005-09-26 | 2009-03-12 | ファーマセット,インコーポレイティド | Modified 4'-nucleosides as antiviral agents |
EP1986603A2 (en) | 2006-01-13 | 2008-11-05 | SurModics, Inc. | Microparticle containing matrices for drug delivery |
WO2007087684A1 (en) | 2006-02-03 | 2007-08-09 | Bionomics Limited | Substituted benzofurans, benzothiophenes, benzoselenophenes and indoles and their use as tubulin polymerisation inhibitors |
AU2007215114A1 (en) | 2006-02-14 | 2007-08-23 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Nucleoside aryl phosphoramidates for the treatment of RNA-dependent RNA viral infection |
US20080166411A1 (en) | 2006-04-10 | 2008-07-10 | Pfizer Inc | Injectable Depot Formulations And Methods For Providing Sustained Release Of Poorly Soluble Drugs Comprising Nanoparticles |
AU2007272839B2 (en) | 2006-07-13 | 2012-05-24 | Achillion Pharmaceuticals, Inc. | 4-amino-4-oxobutanoyl peptides as inhibitors of viral replication |
US8338435B2 (en) | 2006-07-20 | 2012-12-25 | Gilead Sciences, Inc. | Substituted pyrido(3,2-D) pyrimidines and pharmaceutical compositions for treating viral infections |
US7902365B2 (en) | 2006-08-16 | 2011-03-08 | Achillion Pharmaceuticals, Inc. | Method for synthesis of 8-alkoxy-9H-isothiazolo[5,4-B]quinoline-3,4-diones |
US8877780B2 (en) | 2006-08-30 | 2014-11-04 | Celgene Corporation | 5-substituted isoindoline compounds |
BRPI0716092A2 (en) | 2006-08-30 | 2013-09-17 | Celgene Corp | compound or a salt, solvate, or stereoisomer thereof, pharmaceutical composition, method for treating, controlling or preventing a disease or disorder, and, single unit dosage form. |
SI2076260T1 (en) | 2006-09-15 | 2011-05-31 | Celgene Corp | N-methylaminomethyl isoindole compounds and compositions comprising and methods of using the same |
PL2420497T3 (en) | 2006-09-26 | 2016-06-30 | Celgene Corp | 5-substituted quinazolinone derivatives as anti-cancer agents |
US8138164B2 (en) | 2006-10-24 | 2012-03-20 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
CA2667165A1 (en) | 2006-10-24 | 2008-05-02 | Merck & Co., Inc. | Hcv ns3 protease inhibitors |
WO2008051514A2 (en) | 2006-10-24 | 2008-05-02 | Merck & Co., Inc. | Hcv ns3 protease inhibitors |
JP5352464B2 (en) | 2006-10-27 | 2013-11-27 | メルク・シャープ・アンド・ドーム・コーポレーション | HCV NS3 protease inhibitor |
AU2007352397B2 (en) | 2006-12-14 | 2013-09-26 | Gilead Sciences, Inc. | Viral inhibitors |
AU2007338899A1 (en) | 2006-12-20 | 2008-07-03 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Nucleoside cyclic phosphoramidates for the treatment of RNA-dependent RNA viral infection |
US8546420B2 (en) | 2006-12-22 | 2013-10-01 | Merck Sharp & Dohme Corp. | 4, 5-ring annulated indole derivatives for treating or preventing of HCV and related viral infections |
WO2008082484A1 (en) | 2006-12-22 | 2008-07-10 | Schering Corporation | 4,5-ring annulated indole derivatives for treating or preventing of hcv and related viral infections |
WO2008077650A1 (en) | 2006-12-26 | 2008-07-03 | Gilead Sciences, Inc. | Pyrido(3,2-d)pyrimidines useful for treating viral infections |
TW200840584A (en) | 2006-12-26 | 2008-10-16 | Gilead Sciences Inc | Pyrido(3,2-d)pyrimidines useful for treating viral infections |
US8143394B2 (en) | 2006-12-26 | 2012-03-27 | Gilead Sciences, Inc. | Pyrido(3,2-d)pyrimidines useful for treating viral infections |
US7951789B2 (en) | 2006-12-28 | 2011-05-31 | Idenix Pharmaceuticals, Inc. | Compounds and pharmaceutical compositions for the treatment of viral infections |
CA2673649A1 (en) | 2007-01-05 | 2008-07-17 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Nucleoside aryl phosphoramidates for the treatment of rna-dependent rna viral infection |
WO2008100447A2 (en) | 2007-02-09 | 2008-08-21 | Gilead Sciences, Inc. | Nucleoside analogs for antiviral treatment |
EP2125113A2 (en) | 2007-02-26 | 2009-12-02 | Achillion Pharmaceuticals, Inc. | Tertiary amine substituted peptides useful as inhibitors of hcv replication |
KR101791757B1 (en) | 2007-03-20 | 2017-10-30 | 셀진 코포레이션 | 4'-o-substituted isoindoline derivatives and compositions comprising and methods of using the same |
US7964580B2 (en) | 2007-03-30 | 2011-06-21 | Pharmasset, Inc. | Nucleoside phosphoramidate prodrugs |
WO2008122038A1 (en) | 2007-04-02 | 2008-10-09 | President And Fellows Of Harvard College | Regulating autophagy |
WO2008125117A1 (en) | 2007-04-13 | 2008-10-23 | Hvidovre Hospital | Cell culture system of a hepatitis c genotype 3a and 2a chimera |
US8618275B2 (en) | 2007-05-18 | 2013-12-31 | Hvidovre Hospital | Efficient cell culture system for hepatitis C virus genotype 5A |
WO2008147557A2 (en) | 2007-05-22 | 2008-12-04 | Achillion Pharmaceuticals, Inc. | Heteroaryl substituted thiazoles and their use as antiviral agents |
IN2009KN04568A (en) | 2007-06-01 | 2015-08-28 | Univ Princeton | |
AR066820A1 (en) | 2007-06-04 | 2009-09-16 | Novartis Ag | TIADIAZOLIDIN-3 ONA COMPOUNDS |
NZ582096A (en) | 2007-06-29 | 2012-05-25 | Gilead Sciences Inc | Antiviral compounds that inhibit hepatitis c virus (hcv) |
KR20100038417A (en) | 2007-06-29 | 2010-04-14 | 길리애드 사이언시즈, 인코포레이티드 | Antiviral compounds |
AU2008277377B2 (en) | 2007-07-19 | 2013-08-01 | Msd Italia S.R.L. | Macrocyclic compounds as antiviral agents |
US8404845B2 (en) | 2007-08-29 | 2013-03-26 | Merck Sharp & Dohme Corp. | 2,3-substituted azaindole derivatives for treating viral infections |
US20090060867A1 (en) | 2007-08-31 | 2009-03-05 | Idenix Pharmaceuticals, Inc. | Phosphadiazine hcv polymerase inhibitors iii and vi |
JP2010540549A (en) | 2007-09-24 | 2010-12-24 | アキリオン ファーマシューティカルズ,インコーポレーテッド | Urea-containing peptides as viral replication inhibitors |
MY157495A (en) | 2007-09-26 | 2016-06-15 | Celgene Corp | 6-,7-, or 8-substituted quinazolinone derivatives and compositions comprising and methods of using the same |
US20090318380A1 (en) | 2007-11-20 | 2009-12-24 | Pharmasset, Inc. | 2',4'-substituted nucleosides as antiviral agents |
CA2710740C (en) | 2007-12-28 | 2016-07-19 | Shinji Miyoshi | Thienotriazolodiazepine compound as antitumor agent |
RU2490272C2 (en) | 2008-02-04 | 2013-08-20 | Айденикс Фармасьютикалз, Инк. | Macrocyclic serine protease inhibitors |
US20090203709A1 (en) | 2008-02-07 | 2009-08-13 | Abbott Laboratories | Pharmaceutical Dosage Form For Oral Administration Of Tyrosine Kinase Inhibitor |
TWI444384B (en) | 2008-02-20 | 2014-07-11 | Gilead Sciences Inc | Nucleotide analogues and their use in the treatment of malignancies |
KR101806314B1 (en) | 2008-04-03 | 2017-12-07 | 스프링 뱅크 파마슈티칼스, 인크. | Compositions and methods for treating viral infections |
CA2720850A1 (en) | 2008-04-28 | 2009-11-05 | Merck Sharp & Dohme Corp. | Hcv ns3 protease inhibitors |
US20090298882A1 (en) | 2008-05-13 | 2009-12-03 | Muller George W | Thioxoisoindoline compounds and compositions comprising and methods of using the same |
US8106209B2 (en) | 2008-06-06 | 2012-01-31 | Achillion Pharmaceuticals, Inc. | Substituted aminothiazole prodrugs of compounds with anti-HCV activity |
US8173621B2 (en) | 2008-06-11 | 2012-05-08 | Gilead Pharmasset Llc | Nucleoside cyclicphosphates |
US8536187B2 (en) | 2008-07-03 | 2013-09-17 | Gilead Sciences, Inc. | 2,4,6-trisubstituted pyrido(3,2-d)pyrimidines useful for treating viral infections |
DK2310095T3 (en) | 2008-07-22 | 2012-12-10 | Merck Sharp & Dohme | MACROCYCLIC QUINOXALIN COMPOUNDS AS HCV-NS3 PROTEASE INHIBITORS |
AR072938A1 (en) | 2008-08-20 | 2010-09-29 | Southern Res Inst | DERIVATIVES OF PIRIDINE AND PYRIMIDINE AZOSUSTITUIDOS AND ITS USE IN THE TREATMENT OF VIRAL INFECTIONS |
WO2010022125A1 (en) | 2008-08-20 | 2010-02-25 | Schering Corporation | Ethynyl-substituted pyridine and pyrimidine derivatives and their use in treating viral infections |
AR072939A1 (en) | 2008-08-20 | 2010-09-29 | Schering Corp | DERIVATIVES OF PIRIDINE AND PYRIMIDINE REPLACED WITH ETHYLENE AND ITS USE IN THE TREATMENT OF VIRAL INFECTIONS |
TWI409265B (en) | 2008-08-20 | 2013-09-21 | Merck Sharp & Dohme | Substituted pyridine and pyrimidine derivatives and their use in treating viral infections |
US8673288B2 (en) | 2008-09-02 | 2014-03-18 | The Board Of Trustees Of The University Of Illinois | Compositions and methods for inhibiting entry of a hepatic virus |
US9034863B2 (en) | 2008-09-02 | 2015-05-19 | The Board Of Trustees Of The University Of Illinois | Compositions and methods for inhibiting entry of a hepatic virus |
AU2009298177B2 (en) | 2008-10-02 | 2013-02-07 | George Zabrecky | Methods and formulations for treating chronic liver disease |
WO2010037403A1 (en) | 2008-10-03 | 2010-04-08 | Hvidovre Hospital | Hepatitis c virus expressing reporter tagged ns5a protein |
SI2358697T1 (en) | 2008-10-29 | 2016-02-29 | Celgene Corporation | Isoindoline compounds for use in the treatment of cancer. |
EP2350114A1 (en) | 2008-11-20 | 2011-08-03 | Achillion Pharmaceuticals, Inc. | Cyclic carboxamide compounds and analogues thereof as of hepatitis c virus |
CN102245599B (en) | 2008-12-10 | 2014-05-14 | 艾其林医药公司 | New 4-amino-4-oxobutanoyl peptides as inhibitors of viral replication |
AR074882A1 (en) | 2008-12-23 | 2011-02-16 | Pharmasset Inc | NUCLEOSID ANALOGS |
MX2011006891A (en) | 2008-12-23 | 2011-10-06 | Pharmasset Inc | Nucleoside phosphoramidates. |
JP5793084B2 (en) | 2008-12-23 | 2015-10-14 | ギリアド ファーマセット エルエルシー | Synthesis of purine nucleosides |
US20120052041A1 (en) | 2009-02-04 | 2012-03-01 | The Brigham And Women's Hospital, Inc. | Polymeric nanoparticles with enhanced drug-loading and methods of use thereof |
CN102395590A (en) | 2009-02-06 | 2012-03-28 | Rfs制药公司 | Purine nucleoside monophosphate prodrugs for treatment of cancer and viral infections |
JP5690286B2 (en) | 2009-03-04 | 2015-03-25 | イデニク プハルマセウティカルス,インコーポレイテッド | Phosphothiophene and phosphothiazole HCV polymerase inhibitors |
US20120135089A1 (en) | 2009-03-17 | 2012-05-31 | Stockwell Brent R | E3 ligase inhibitors |
US20100261711A1 (en) | 2009-03-20 | 2010-10-14 | Wisys Technology Foundation | Selective anticonvulsant agents and their uses |
SG10201402969QA (en) | 2009-03-27 | 2014-09-26 | Merck Sharp & Dohme | Inhibitors of hepatitis c virus replication |
BRPI1015079A2 (en) | 2009-04-03 | 2015-09-01 | Achillion Pharmaceuticals Inc | Hydroxythienoquinolones and related compounds as antiinfectives |
JP2012523419A (en) | 2009-04-08 | 2012-10-04 | イデニク プハルマセウティカルス,インコーポレイテッド | Macrocyclic serine protease inhibitor |
DK2421879T3 (en) | 2009-04-22 | 2013-11-25 | Acad Of Science Czech Republic | New 7-deazapurine nucleotides for therapeutic applications |
JP2012526834A (en) | 2009-05-12 | 2012-11-01 | シェーリング コーポレイション | Condensed tricyclic aryl compounds useful for the treatment of viral diseases |
WO2010132601A1 (en) | 2009-05-13 | 2010-11-18 | Gilead Sciences, Inc. | Antiviral compounds |
US10952965B2 (en) | 2009-05-15 | 2021-03-23 | Baxter International Inc. | Compositions and methods for drug delivery |
TWI583692B (en) | 2009-05-20 | 2017-05-21 | 基利法瑪席特有限責任公司 | Nucleoside phosphoramidates |
US8618076B2 (en) | 2009-05-20 | 2013-12-31 | Gilead Pharmasset Llc | Nucleoside phosphoramidates |
EP2435424B1 (en) | 2009-05-29 | 2015-01-21 | Merck Sharp & Dohme Corp. | Antiviral compounds composed of three linked aryl moieties to treat diseases such as hepatitis c |
AU2010253790A1 (en) | 2009-05-29 | 2011-12-15 | Merck Sharp & Dohme Corp. | Antiviral compounds composed of three aligned aryl moieties to treat diseases such as Hepatitis C |
JP5841531B2 (en) | 2009-07-21 | 2016-01-13 | ギリアード サイエンシーズ, インコーポレイテッド | Inhibitors of Flaviviridae virus |
EP2459582B1 (en) | 2009-07-30 | 2015-05-27 | Merck Sharp & Dohme Corp. | Hepatitis c virus ns3 protease inhibitors |
WO2011017389A1 (en) | 2009-08-05 | 2011-02-10 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors useful against viral infections, particularly hcv |
CA2770338A1 (en) | 2009-08-27 | 2011-03-03 | Merck Sharp & Dohme Corp. | Processes for preparing protease inhibitors of hepatitis c virus |
WO2011031669A1 (en) | 2009-09-09 | 2011-03-17 | Gilead Sciences, Inc. | Inhibitors of flaviviridae viruses |
SG10201406813RA (en) | 2009-10-22 | 2014-11-27 | Gilead Sciences Inc | Derivatives of purine or deazapurine useful for the treatment of (inter alia) viral infections |
US8927484B2 (en) | 2009-12-03 | 2015-01-06 | Gilead Sciences, Inc. | Antiviral compounds |
US8476225B2 (en) | 2009-12-04 | 2013-07-02 | Gilead Sciences, Inc. | Antiviral compounds |
CA2784748A1 (en) | 2009-12-18 | 2011-06-23 | Idenix Pharmaceuticals, Inc. | 5,5-fused arylene or heteroarylene hepatitis c virus inhibitors |
US20130029904A1 (en) | 2009-12-18 | 2013-01-31 | Boehringer Ingelheim International Gmbh | Hcv combination therapy |
CA2785567C (en) | 2010-01-15 | 2018-03-27 | Gilead Sciences, Inc. | Inhibitors of flaviviridae viruses |
JP5777223B2 (en) | 2010-01-15 | 2015-09-09 | ギリアード サイエンシーズ, インコーポレイテッド | Inhibitors of Flaviviridae virus |
AU2011210765A1 (en) | 2010-01-28 | 2012-09-13 | President And Fellows Of Harvard College | Compositions and methods for enhancing proteasome activity |
WO2011097218A1 (en) | 2010-02-02 | 2011-08-11 | Wayne State University | Anti-cancer therapeutic agents |
US20130071349A1 (en) | 2010-03-02 | 2013-03-21 | Allergan, Inc. | Biodegradable polymers for lowering intraocular pressure |
US8609635B2 (en) | 2010-03-09 | 2013-12-17 | Merck Sharp & Dohme Corp. | Fused tricyclic silyl compounds and methods of use thereof for the treatment of viral diseases |
US8563530B2 (en) | 2010-03-31 | 2013-10-22 | Gilead Pharmassel LLC | Purine nucleoside phosphoramidate |
MX2012011222A (en) | 2010-04-01 | 2013-01-18 | Centre Nat Rech Scient | Compounds and pharmaceutical compositions for the treatment of viral infections. |
US9125904B1 (en) | 2010-05-11 | 2015-09-08 | Achillion Pharmaceuticals, Inc. | Biphenyl imidazoles and related compounds useful for treating HCV infections |
HUE031073T2 (en) | 2010-05-14 | 2017-06-28 | Dana Farber Cancer Inst Inc | Thienotriazolodiazepine compounds for treating neoplasia |
CA2797872A1 (en) | 2010-05-21 | 2011-11-24 | Gilead Sciences, Inc. | Heterocyclic flaviviridae virus inhibitors |
WO2011153310A1 (en) | 2010-06-02 | 2011-12-08 | Trius Therapeutics | Dihydrofolate reductase inhibitors |
US8703810B2 (en) | 2010-06-10 | 2014-04-22 | Seragon Pharmaceuticals, Inc. | Estrogen receptor modulators and uses thereof |
US8853423B2 (en) | 2010-06-17 | 2014-10-07 | Seragon Pharmaceuticals, Inc. | Indane estrogen receptor modulators and uses thereof |
CN105481866A (en) | 2010-06-24 | 2016-04-13 | 吉里德科学公司 | Pyrazolo [1, 5 -a] pyrimidines as antiviral agents |
IN2012MN02896A (en) | 2010-06-24 | 2015-06-12 | Panmed Ltd | |
SG186389A1 (en) | 2010-06-30 | 2013-01-30 | Univ Brandeis | Small-molecule-targeted protein degradation |
ES2524398T3 (en) | 2010-07-19 | 2014-12-09 | Gilead Sciences, Inc. | Methods for the preparation of diastereomerically pure phosphoramidate prodrugs |
CA2809261A1 (en) | 2010-08-26 | 2012-03-01 | Rfs Pharma, Llc | Potent and selective inhibitors of hepatitis c virus |
GB2483736B (en) | 2010-09-16 | 2012-08-29 | Aragon Pharmaceuticals Inc | Estrogen receptor modulators and uses thereof |
WO2012040124A1 (en) | 2010-09-22 | 2012-03-29 | Alios Biopharma, Inc. | Azido nucleosides and nucleotide analogs |
MX2013003153A (en) | 2010-09-22 | 2013-05-01 | Alios Biopharma Inc | Substituted nucleotide analogs. |
AU2011314168A1 (en) | 2010-09-29 | 2013-04-04 | Merck Sharp & Dohme Corp. | Fused tetracycle derivatives and methods of use thereof for the treatment of viral diseases |
US10005750B2 (en) | 2010-10-06 | 2018-06-26 | J-Pharma Co., Ltd. | Developing potent urate transporter inhibitors: compounds designed for their uricosuric action |
SG10201509456SA (en) | 2010-11-17 | 2015-12-30 | Gilead Pharmasset Llc | Antiviral compounds |
ES2716158T3 (en) | 2010-11-30 | 2019-06-10 | Gilead Pharmasset Llc | 2'-spiro-nucleotides for the treatment of hepatitis C |
WO2012075456A1 (en) | 2010-12-02 | 2012-06-07 | Constellation Pharmaceuticals | Bromodomain inhibitors and uses thereof |
CN103502275A (en) | 2010-12-07 | 2014-01-08 | 耶鲁大学 | Small-molecule hydrophobic tagging of fusion proteins and induced degradation of same |
UY33775A (en) | 2010-12-10 | 2012-07-31 | Gilead Sciences Inc | MACROCYCLIC INHIBITORS OF VIRUS FLAVIVIRIDAE, PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND AND THEIR USES |
WO2012079022A1 (en) | 2010-12-10 | 2012-06-14 | Concert Pharmaceuticals, Inc. | Substituted dioxopiperidinyl phthalimide derivatives |
US9120818B2 (en) | 2010-12-14 | 2015-09-01 | Merck Sharp & Dohme Corp. | Process and intermediates for preparing macrolactams |
TW201307334A (en) | 2010-12-17 | 2013-02-16 | Cocrystal Discovery Inc | Inhibitors of hepatitis C virus polymerase |
EP2655392B1 (en) | 2010-12-22 | 2018-04-18 | Alios Biopharma, Inc. | Cyclic nucleotide analogs |
CA2819299A1 (en) | 2010-12-24 | 2012-06-28 | Merck Sharp & Dohme B.V. | N-substituted azetidine derivatives |
US9353100B2 (en) | 2011-02-10 | 2016-05-31 | Idenix Pharmaceuticals Llc | Macrocyclic serine protease inhibitors, pharmaceutical compositions thereof, and their use for treating HCV infections |
BRPI1100318A2 (en) | 2011-02-18 | 2013-05-21 | Univ Estadual Paulista Jelio De Mesquita Filho | A process for obtaining compounds derived from steroidal anti-inflammatory drugs (s), pharmaceutical compositions containing such compounds and their uses in the treatment of inflammatory diseases. |
US8835456B1 (en) | 2011-03-18 | 2014-09-16 | Achillion Pharmaceuticals, Inc. | NS5A inhibitors useful for treating HCV |
CN103842369A (en) | 2011-03-31 | 2014-06-04 | 埃迪尼克斯医药公司 | Compounds and pharmaceutical compositions for the treatment of viral infections |
WO2012142085A1 (en) | 2011-04-13 | 2012-10-18 | Merck Sharp & Dohme Corp. | 2'-substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases |
CA2832449A1 (en) | 2011-04-13 | 2012-10-18 | Vinay GIRIJAVALLABHAN | 2'-cyano substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases |
EP2697242B1 (en) | 2011-04-13 | 2018-10-03 | Merck Sharp & Dohme Corp. | 2'-azido substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases |
NO2694640T3 (en) | 2011-04-15 | 2018-03-17 | ||
ES2584418T3 (en) | 2011-05-27 | 2016-09-27 | Achillion Pharmaceuticals, Inc. | Aliphanes, cyclophanes, heteraphans, heterophanes, hetero-heteraphans and substituted metallocenes useful for the treatment of HCV infections |
US20150197497A1 (en) | 2011-06-24 | 2015-07-16 | Dana-Farber Cancer Institute, Inc. | Selective inhibitors of histone deacetylase isoform 6 and methods thereof |
KR20140064765A (en) | 2011-06-30 | 2014-05-28 | 스텔라 에이피에스 | Hcv combination therapy |
CA2840445A1 (en) | 2011-07-13 | 2013-01-17 | Gilead Sciences, Inc. | Thiophen-2-carboxylic acid derivatives useful as inhibitors of flaviviridae viruses |
MX2014001945A (en) | 2011-08-19 | 2014-03-27 | Merck Sharp & Dohme | Process and intermediates for preparing macrolactams. |
WO2013033900A1 (en) | 2011-09-08 | 2013-03-14 | Merck Sharp & Dohme Corp. | Tetracyclic heterocycle compounds and methods of use thereof for the treatment of viral diseases |
EP2755985B1 (en) | 2011-09-12 | 2017-11-01 | Idenix Pharmaceuticals LLC | Compounds and pharmaceutical compositions for the treatment of viral infections |
US8664386B2 (en) | 2011-10-07 | 2014-03-04 | Gilead Sciences, Inc. | Methods for preparing anti-viral nucleotide analogs |
CA2847083A1 (en) | 2011-10-10 | 2013-04-18 | F. Hoffmann-La Roche Ag | Antiviral compounds |
TW201331221A (en) | 2011-10-14 | 2013-08-01 | Idenix Pharmaceuticals Inc | Substituted 3',5'-cyclic phosphates of purine nucleotide compounds and pharmaceutical compositions for the treatment of viral infections |
EP2768799B1 (en) | 2011-10-17 | 2019-08-07 | Biotheryx Inc. | Substituted biaryl alkyl amides |
WO2013074386A2 (en) | 2011-11-15 | 2013-05-23 | Merck Sharp & Dohme Corp. | Hcv ns3 protease inhibitors |
ES2687291T3 (en) | 2011-11-16 | 2018-10-24 | Gilead Pharmasset Llc | Condensed Imidazolylimidazoles as antiviral compounds |
US8889159B2 (en) | 2011-11-29 | 2014-11-18 | Gilead Pharmasset Llc | Compositions and methods for treating hepatitis C virus |
MX357496B (en) | 2011-12-14 | 2018-07-11 | Seragon Pharmaceuticals Inc | Fluorinated estrogen receptor modulators and uses thereof. |
WO2013087743A1 (en) | 2011-12-16 | 2013-06-20 | F. Hoffmann-La Roche Ag | Inhibitors of hcv ns5a |
KR20140103335A (en) | 2011-12-16 | 2014-08-26 | 올레마 파마슈티컬스 인코포레이티드 | Novel benzopyran compounds, compositions and uses thereof |
BR112014013661B1 (en) | 2011-12-20 | 2020-10-27 | Riboscience Llc. | 2,4-DIFLUORO-2-METHIL NUCLEOSIDE DERIVATIVES REPLACED AS HCV-RNA REPLICATION INHIBITORS |
JP5977837B2 (en) | 2011-12-21 | 2016-08-24 | ノヴィラ・セラピューティクス・インコーポレイテッド | Hepatitis B antiviral agent |
US8980865B2 (en) | 2011-12-22 | 2015-03-17 | Alios Biopharma, Inc. | Substituted nucleotide analogs |
BR112014014740B1 (en) | 2011-12-22 | 2021-08-24 | Alios Biopharma, Inc | NUCLEOSIDE COMPOUNDS, NUCLEOTIDES AND THEIR ANALOGUES, THEIR USE AND PHARMACEUTICAL COMPOSITION |
WO2013096681A1 (en) | 2011-12-22 | 2013-06-27 | Gilead Sciences, Inc. | Pyrazolo[1,5-a]pyrimidines as antiviral agents |
JP2015508414A (en) | 2012-01-12 | 2015-03-19 | イエール ユニバーシティ | Compounds and methods for enhanced degradation of target proteins and other polypeptides by E3 ubiquitin ligase |
US9040479B2 (en) | 2012-01-12 | 2015-05-26 | Cocrystal Pharma, Inc. | HCV NS3 protease inhibitors |
WO2013106646A2 (en) | 2012-01-12 | 2013-07-18 | Yale University | Compounds and methods for the inhibition of vcb e3 ubiquitin ligase |
EP2812326A1 (en) | 2012-02-10 | 2014-12-17 | Lupin Limited | Antiviral compounds with a dibenzooxaheterocycle moiety |
BR112014015582A8 (en) | 2012-02-24 | 2017-07-04 | Hoffmann La Roche | antiviral compounds |
CN104334570B (en) | 2012-03-21 | 2017-06-06 | 艾丽奥斯生物制药有限公司 | The method for preparing the nucleotide analog of substitution |
NZ630805A (en) | 2012-03-22 | 2016-01-29 | Alios Biopharma Inc | Pharmaceutical combinations comprising a thionucleotide analog |
US20140107025A1 (en) | 2012-04-16 | 2014-04-17 | Jade Therapeutics, Llc | Ocular drug delivery system |
SI2838900T1 (en) | 2012-04-17 | 2019-10-30 | Gilead Sciences Inc | Compounds and methods for antiviral treatment |
EP2846784A4 (en) | 2012-05-11 | 2016-03-09 | Univ Yale | Compounds useful for promoting protein degradation and methods using same |
US9079887B2 (en) | 2012-05-16 | 2015-07-14 | Gilead Sciences, Inc. | Antiviral compounds |
RU2014145121A (en) | 2012-05-22 | 2016-07-10 | Зэ Юниверсити Оф Норд Каролина Эт Чапел Хилл | PYRIMIDINE COMPOUNDS FOR TREATING A MALIGNANT TUMOR |
EP2852605B1 (en) | 2012-05-22 | 2018-01-31 | Idenix Pharmaceuticals LLC | 3',5'-cyclic phosphate prodrugs for hcv infection |
EP2852604B1 (en) | 2012-05-22 | 2017-04-12 | Idenix Pharmaceuticals LLC | 3',5'-cyclic phosphoramidate prodrugs for hcv infection |
US8969588B2 (en) | 2012-06-05 | 2015-03-03 | Gilead Pharmasset Llc | Solid forms of an antiviral compound |
US9056860B2 (en) | 2012-06-05 | 2015-06-16 | Gilead Pharmasset Llc | Synthesis of antiviral compound |
KR20150040265A (en) | 2012-06-08 | 2015-04-14 | 길리애드 사이언시즈, 인코포레이티드 | Macrocyclic inhibitors of flaviviridae viruses |
AR091279A1 (en) | 2012-06-08 | 2015-01-21 | Gilead Sciences Inc | MACROCICLIC INHIBITORS OF VIRUS FLAVIVIRIDAE |
KR20150040266A (en) | 2012-06-08 | 2015-04-14 | 길리애드 사이언시즈, 인코포레이티드 | Macrocyclic inhibitors of flaviviridae viruses |
UA119315C2 (en) | 2012-07-03 | 2019-06-10 | Гіліад Фармассет Елелсі | Inhibitors of hepatitis c virus |
CN104145514B (en) | 2012-08-01 | 2018-03-13 | 华为技术有限公司 | Method, apparatus and system for synchronization |
TW201408669A (en) | 2012-08-08 | 2014-03-01 | Merck Sharp & Dohme | HCV NS3 protease inhibitors |
US8759544B2 (en) | 2012-08-17 | 2014-06-24 | Gilead Sciences, Inc. | Synthesis of an antiviral compound |
US8927741B2 (en) | 2012-08-17 | 2015-01-06 | Gilead Sciences, Inc. | Synthesis of an antiviral compound |
HUE031400T2 (en) | 2012-08-28 | 2017-07-28 | Janssen Sciences Ireland Uc | Fused bicyclic sulfamoyl derivatives and the use thereof as medicaments for the treatment of hepatitis b |
CN104822370A (en) | 2012-09-17 | 2015-08-05 | 佰恩德治疗股份有限公司 | Therapeutic nanoparticles comprising a therapeutic agent and methods of making and using same |
MX2015003665A (en) | 2012-09-20 | 2016-03-08 | Akina Inc | Biodegradable microcapsules containing filling material. |
EP2909209B1 (en) | 2012-10-17 | 2022-08-03 | Merck Sharp & Dohme LLC | 2'-cyano substituted nucleoside derivatives and methods of use thereof for treatment of viral diseases |
US9758522B2 (en) | 2012-10-19 | 2017-09-12 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged small molecules as inducers of protein degradation |
RU2019131148A (en) | 2012-11-01 | 2019-11-08 | Инфинити Фармасьютикалз, Инк. | TREATMENT OF MALIGNANT TUMORS USING MODULATORS OF PI3-KINASE ISOFORM |
EP2917340A1 (en) | 2012-11-07 | 2015-09-16 | Gilead Sciences, Inc. | Hcv genotype 6 replicons |
WO2014085225A1 (en) | 2012-11-27 | 2014-06-05 | The University Of North Carolina At Chapel Hill | Pyrimidine compounds for the treatment of cancer |
WO2014099941A1 (en) | 2012-12-19 | 2014-06-26 | Idenix Pharmaceuticals, Inc. | 4'-fluoro nucleosides for the treatment of hcv |
SG11201504554UA (en) | 2012-12-21 | 2015-07-30 | Alios Biopharma Inc | Substituted nucleosides, nucleotides and analogs thereof |
US9233974B2 (en) | 2012-12-21 | 2016-01-12 | Gilead Sciences, Inc. | Antiviral compounds |
ES2753548T3 (en) | 2012-12-21 | 2020-04-13 | Gilead Sciences Inc | Polycyclic carbamoyl-pyridone compounds and their pharmaceutical use |
WO2014121418A1 (en) | 2013-02-07 | 2014-08-14 | Merck Sharp & Dohme Corp. | Tetracyclic heterocycle compounds and methods of use thereof for the treatment of hepatitis c |
WO2014121416A1 (en) | 2013-02-07 | 2014-08-14 | Merck Sharp & Dohme Corp. | Tetracyclic heterocycle compounds and methods of use thereof for the treatment of hepatitis c |
US9309275B2 (en) | 2013-03-04 | 2016-04-12 | Idenix Pharmaceuticals Llc | 3′-deoxy nucleosides for the treatment of HCV |
WO2014137930A1 (en) | 2013-03-04 | 2014-09-12 | Idenix Pharmaceuticals, Inc. | Thiophosphate nucleosides for the treatment of hcv |
MX2015010790A (en) | 2013-03-05 | 2015-11-26 | Hoffmann La Roche | N-heteroaryl substituted aniline derivatives as hcv-antivirals. |
US10723753B2 (en) | 2013-03-13 | 2020-07-28 | Dana-Farber Cancer Institute, Inc. | Ras inhibitors and uses thereof |
CA2905433A1 (en) | 2013-03-14 | 2014-09-25 | Achillion Pharmaceuticals, Inc. | Novel processes for producing sovaprevir |
WO2014140077A1 (en) | 2013-03-14 | 2014-09-18 | Glaxosmithkline Intellectual Property (No.2) Limited | Furopyridines as bromodomain inhibitors |
CN105228649B (en) | 2013-03-14 | 2019-01-18 | 雅培制药有限公司 | HCV Ag-Ab combination measurement is with method and used in composition therein |
WO2014145507A1 (en) | 2013-03-15 | 2014-09-18 | Achillion Pharmaceuticals, Inc. | A process for making a 4-amino-4-oxobutanoyl peptide cyclic analogue, an inhibitor of viral replication, and intermediates thereof |
JP2016520532A (en) | 2013-03-15 | 2016-07-14 | ホワイトヘッド・インスティテュート・フォー・バイオメディカル・リサーチ | Benzimidazole derivatives and uses thereof |
US9227952B2 (en) | 2013-03-15 | 2016-01-05 | Achillion Pharmaceuticals, Inc. | Sovaprevir polymorphs and methods of manufacture thereof |
US9085607B2 (en) | 2013-03-15 | 2015-07-21 | Achillion Pharmaceuticals, Inc. | ACH-0142684 sodium salt polymorph, composition including the same, and method of manufacture thereof |
WO2014165542A1 (en) | 2013-04-01 | 2014-10-09 | Idenix Pharmaceuticals, Inc. | 2',4'-fluoro nucleosides for the treatment of hcv |
EP2981248B1 (en) | 2013-04-01 | 2020-09-02 | Allergan, Inc. | Microsphere drug delivery system for sustained intraocular release |
EP2996696A4 (en) | 2013-05-16 | 2016-12-21 | Riboscience Llc | 4'-azido, 3'-deoxy-3'-fluoro substituted nucleoside derivatives |
CN105229004B (en) | 2013-05-28 | 2017-05-03 | 阿斯利康(瑞典)有限公司 | Chemical compounds |
CN105451735B (en) | 2013-06-19 | 2019-01-11 | 西拉根制药公司 | Azetidine estrogenic agents and its purposes |
WO2014203129A1 (en) | 2013-06-19 | 2014-12-24 | Olema Pharmaceuticals, Inc. | Combinations of benzopyran compounds, compositions and uses thereof |
WO2014203132A1 (en) | 2013-06-19 | 2014-12-24 | Olema Pharmaceuticals, Inc. | Substituted benzopyran compounds, compositions and uses thereof |
BR112015031903A8 (en) | 2013-06-19 | 2019-12-31 | Seragon Pharmaceuticals Inc | compound, pharmaceutically acceptable salt, pharmaceutical composition and use of a compound |
WO2014205593A1 (en) | 2013-06-24 | 2014-12-31 | Merck Sharp & Dohme Corp. | Substituted benzofuran compounds and methods of use thereof for treatment of viral diseases |
FR3008978A1 (en) | 2013-07-23 | 2015-01-30 | Servier Lab | "NOVEL INDOLE AND PYRROLE DERIVATIVES, PROCESS FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM" |
CN105555786A (en) | 2013-07-23 | 2016-05-04 | 拜耳制药股份公司 | Substituted dihydropyrido[3,4-b]pyrazinones as dual inhibitors of bet proteins and polo-like kinases |
AU2014298051B2 (en) | 2013-07-31 | 2018-11-15 | Zenith Epigenetics Ltd. | Novel quinazolinones as bromodomain inhibitors |
CN103421061A (en) | 2013-08-14 | 2013-12-04 | 中国药科大学 | Lenalidomide derivative and preparation method and pharmaceutical application thereof |
US20150051208A1 (en) | 2013-08-14 | 2015-02-19 | Boehringer Ingelheim International Gmbh | Pyridinones |
EP3778603A1 (en) | 2013-09-12 | 2021-02-17 | Janssen BioPharma, Inc. | 7,8-dihydro-3h-pyrazino[1,2-b]pyridazine-3,5(6h)-dione compounds and uses thereof |
WO2015057945A1 (en) | 2013-10-18 | 2015-04-23 | Indiana University Research And Technology Corporation | Hepatitis b viral assembly effectors |
US9428513B2 (en) | 2013-11-07 | 2016-08-30 | Boehringer Ingelheim International Gmbh | Triazolopyrazine |
US9115113B2 (en) | 2013-11-14 | 2015-08-25 | Novira Therapeutics, Inc. | Azepane derivatives and methods of treating hepatitis B infections |
RS61519B1 (en) | 2013-11-18 | 2021-03-31 | Forma Therapeutics Inc | Tetrahydroquinoline compositions as bet bromodomain inhibitors |
WO2015081203A1 (en) | 2013-11-26 | 2015-06-04 | Incyte Corporation | Bicyclic heterocycles as bet protein inhibitors |
FR3015483B1 (en) | 2013-12-23 | 2016-01-01 | Servier Lab | NOVEL THIENOPYRIMIDINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME |
JP6351306B2 (en) | 2014-03-06 | 2018-07-04 | キヤノン株式会社 | Image processing apparatus, image processing apparatus control method, and program |
US10183936B2 (en) | 2014-03-13 | 2019-01-22 | Indiana University Research And Technology Corporation | Hepatitis B core protein allosteric modulators |
KR20160124909A (en) | 2014-03-13 | 2016-10-28 | 에프. 호프만-라 로슈 아게 | Therapeutic combinations with estrogen receptor modulators |
CN106132968B (en) | 2014-04-09 | 2019-04-05 | 康佳诺医疗科技发展有限公司 | It is a kind of for prevent or treating cancer inhibition bromine structural domain compound and containing the pharmaceutical composition of the compound |
KR20220101015A (en) | 2014-04-14 | 2022-07-18 | 아비나스 오퍼레이션스, 인코포레이티드 | Imide-based modulators of proteolysis and associated methods of use |
US9428515B2 (en) | 2014-05-09 | 2016-08-30 | Boehringer Ingelheim International Gmbh | Benzimidazole derivatives |
EA201650031A1 (en) * | 2014-05-15 | 2017-06-30 | Итеос Терапьютик | DERIVATIVES PYRROLIDIN-2,5-DIONA, PHARMACEUTICAL COMPOSITIONS AND METHODS OF APPLICATION AS IDO1 INHIBITORS |
TW201609751A (en) | 2014-07-01 | 2016-03-16 | 武田藥品工業股份有限公司 | Heterocyclic compound |
US20160022642A1 (en) | 2014-07-25 | 2016-01-28 | Yale University | Compounds Useful for Promoting Protein Degradation and Methods Using Same |
WO2016022890A1 (en) | 2014-08-08 | 2016-02-11 | Duquesne University Of The Holy Spirit | Pyrimidine compounds and pyrimido indole compounds and methods of use |
US10071164B2 (en) | 2014-08-11 | 2018-09-11 | Yale University | Estrogen-related receptor alpha based protac compounds and associated methods of use |
JO3474B1 (en) | 2014-08-29 | 2020-07-05 | Amgen Inc | Tetrahydronaphthalene derivatives that inhibit mcl-1 protein |
KR101520275B1 (en) | 2014-09-05 | 2015-05-14 | 주식회사 보승엘티디 | Cosmetic brush case |
WO2016065139A1 (en) | 2014-10-24 | 2016-04-28 | Fl Therapeutics Llc | 3-substituted piperidine-2, 6-diones and non-covalent complexes with albumin |
CN107108611B (en) | 2014-12-18 | 2020-09-25 | 豪夫迈·罗氏有限公司 | Tetrahydro-pyrido [3,4-b ] indole estrogen receptor modulators and uses thereof |
US9694084B2 (en) | 2014-12-23 | 2017-07-04 | Dana-Farber Cancer Institute, Inc. | Methods to induce targeted protein degradation through bifunctional molecules |
JP6815318B2 (en) | 2014-12-23 | 2021-01-20 | ダナ−ファーバー キャンサー インスティテュート,インコーポレイテッド | How to Induce Targeted Proteolysis by Bifunctional Molecules |
EP3247708A4 (en) | 2015-01-20 | 2018-09-12 | Arvinas, Inc. | Compounds and methods for the targeted degradation of the androgen receptor |
GB201504314D0 (en) | 2015-03-13 | 2015-04-29 | Univ Dundee | Small molecules |
CN108601764A (en) | 2015-03-18 | 2018-09-28 | 阿尔维纳斯股份有限公司 | The Compounds and methods for of enhancing degradation for target protein |
GB201506871D0 (en) | 2015-04-22 | 2015-06-03 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
MX2017014567A (en) | 2015-05-22 | 2018-06-28 | Biotheryx Inc | Compounds targeting proteins, compositions, methods, and uses thereof. |
KR20240119196A (en) | 2015-06-04 | 2024-08-06 | 아비나스 오퍼레이션스, 인코포레이티드 | Imide-based modulators of proteolysis and associated methods of use |
US20180147202A1 (en) | 2015-06-05 | 2018-05-31 | Arvinas, Inc. | TANK-BINDING KINASE-1 PROTACs AND ASSOCIATED METHODS OF USE |
FR3037959B1 (en) | 2015-06-23 | 2017-08-04 | Servier Lab | NOVEL BICYCLIC DERIVATIVES, PROCESS FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME |
WO2017007612A1 (en) | 2015-07-07 | 2017-01-12 | Dana-Farber Cancer Institute, Inc. | Methods to induce targeted protein degradation through bifunctional molecules |
CA2988430A1 (en) | 2015-07-10 | 2017-01-19 | Arvinas, Inc. | Mdm2-based modulators of proteolysis and associated methods of use |
WO2017011590A1 (en) | 2015-07-13 | 2017-01-19 | Arvinas, Inc. | Alanine-based modulators of proteolysis and associated methods of use |
WO2017024317A2 (en) | 2015-08-06 | 2017-02-09 | Dana-Farber Cancer Institute, Inc. | Methods to induce targeted protein degradation through bifunctional molecules |
CA2994969A1 (en) | 2015-08-06 | 2017-02-09 | Dana-Farber Cancer Institute, Inc. | Targeted protein degradation to attenuate adoptive t-cell therapy associated adverse inflammatory responses |
US10772962B2 (en) | 2015-08-19 | 2020-09-15 | Arvinas Operations, Inc. | Compounds and methods for the targeted degradation of bromodomain-containing proteins |
CA3002709A1 (en) | 2015-11-02 | 2017-05-11 | Yale University | Proteolysis targeting chimera compounds and methods of preparing and using same |
AU2017232906B2 (en) | 2016-03-16 | 2022-03-31 | H. Lee Moffitt Cancer Center & Research Institute, Inc. | Small molecules against cereblon to enhance effector T cell function |
US20170281784A1 (en) | 2016-04-05 | 2017-10-05 | Arvinas, Inc. | Protein-protein interaction inducing technology |
US11192898B2 (en) | 2016-04-06 | 2021-12-07 | The Regents Of The University Of Michigan | MDM2 protein degraders |
EP3440082A1 (en) | 2016-04-06 | 2019-02-13 | The Regents of The University of Michigan | Monofunctional intermediates for ligand-dependent target protein degradation |
EP3442976B1 (en) | 2016-04-12 | 2022-07-20 | The Regents of The University of Michigan | Bet protein degraders |
WO2017197240A1 (en) | 2016-05-12 | 2017-11-16 | The Regents Of The University Of Michigan | Ash1l inhibitors and methods of treatment therewith |
WO2017201069A1 (en) | 2016-05-18 | 2017-11-23 | Biotheryx, Inc. | Oxoindoline derivatives as protein function modulators |
PL3458101T3 (en) | 2016-05-20 | 2021-05-31 | F. Hoffmann-La Roche Ag | Protac antibody conjugates and methods of use |
US10646488B2 (en) | 2016-07-13 | 2020-05-12 | Araxes Pharma Llc | Conjugates of cereblon binding compounds and G12C mutant KRAS, HRAS or NRAS protein modulating compounds and methods of use thereof |
CA3032136A1 (en) | 2016-07-28 | 2018-02-01 | Mayo Foundation For Medical Education And Research | Small molecule activators of parkin enzyme function |
CN106478639B (en) | 2016-09-05 | 2018-09-18 | 郑州大学 | LSD1 inhibitor, preparation method and the application of 1,2,4-triazole of pyrimido |
ES2857743T3 (en) | 2016-09-13 | 2021-09-29 | Univ Michigan Regents | 1,4-diazepines fused as BET protein degraders |
JP6961684B2 (en) | 2016-09-13 | 2021-11-05 | ザ リージェンツ オブ ザ ユニヴァシティ オブ ミシガン | Condensation 1,4-oxazepine as a BET proteolytic agent |
GB2554071A (en) | 2016-09-14 | 2018-03-28 | Univ Dundee | Small molecules |
ES2975558T3 (en) | 2016-09-15 | 2024-07-09 | Arvinas Inc | Indole derivatives as estrogen receptor degraders |
MX2019004278A (en) | 2016-10-11 | 2019-08-05 | Arvinas Inc | Compounds and methods for the targeted degradation of androgen receptor. |
WO2018085247A1 (en) | 2016-11-01 | 2018-05-11 | Cornell University | Compounds for malt1 degradation |
CA3042260C (en) | 2016-11-01 | 2023-10-03 | Arvinas, Inc. | Tau-protein targeting protacs and associated methods of use |
PL3689868T3 (en) | 2016-12-01 | 2024-03-11 | Arvinas Operations, Inc. | Tetrahydronaphthalene and tetrahydroisoquinoline derivatives as estrogen receptor degraders |
CA3043938A1 (en) | 2016-12-21 | 2018-06-28 | Biotheryx, Inc. | Thienopyrrole derivatives for use in targeting proteins, compositions, methods, and uses thereof |
BR112019012682A2 (en) | 2016-12-23 | 2019-12-17 | Arvinas Operations Inc | chimeric molecules targeting egfr proteolysis and associated methods of use |
US10806737B2 (en) | 2016-12-23 | 2020-10-20 | Arvinas Operations, Inc. | Compounds and methods for the targeted degradation of fetal liver kinase polypeptides |
CA3047784A1 (en) | 2016-12-23 | 2018-06-28 | Arvinas Operations, Inc. | Compounds and methods for the targeted degradation of rapidly accelerated fibrosarcoma polypeptides |
US11191741B2 (en) | 2016-12-24 | 2021-12-07 | Arvinas Operations, Inc. | Compounds and methods for the targeted degradation of enhancer of zeste homolog 2 polypeptide |
AU2018211975B2 (en) | 2017-01-26 | 2022-05-26 | Arvinas Operations, Inc. | Modulators of estrogen receptor proteolysis and associated methods of use |
AU2018215212B2 (en) | 2017-01-31 | 2022-06-02 | Arvinas Operations, Inc. | Cereblon ligands and bifunctional compounds comprising the same |
WO2018169777A1 (en) | 2017-03-14 | 2018-09-20 | Biotheryx, Inc. | Compounds targeting proteins, compositions, methods, and uses thereof |
WO2018183411A1 (en) | 2017-03-28 | 2018-10-04 | The Regents Of The University Of Michigan | Small molecule dcn1 inhibitors and therapeutic methods using the same |
CN110740996B (en) | 2017-04-10 | 2024-01-09 | 密执安大学评议会 | Covalent small molecule DCN1 inhibitors and methods of treatment using the same |
CA3059671A1 (en) | 2017-04-14 | 2018-10-18 | University Of Dundee | Small molecules |
CA3109981A1 (en) | 2018-09-07 | 2020-03-12 | Arvinas Operations, Inc. | Polycyclic compounds and methods for the targeted degradation of rapidly accelerated fibrosarcoma polypeptides |
-
2017
- 2017-05-10 EP EP17796809.6A patent/EP3455218A4/en active Pending
- 2017-05-10 WO PCT/US2017/032041 patent/WO2017197046A1/en unknown
- 2017-05-10 CN CN201780040458.1A patent/CN109641874A/en active Pending
-
2018
- 2018-11-09 US US16/186,341 patent/US10849982B2/en active Active
-
2020
- 2020-11-30 US US17/107,781 patent/US11992531B2/en active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007031791A1 (en) * | 2005-09-16 | 2007-03-22 | Arrow Therapeutics Limited | Biphenyl derivatives and their use in treating hepatitis c |
WO2013089278A1 (en) * | 2011-12-14 | 2013-06-20 | Taiho Pharmaceutical Co., Ltd. | Recombinant prpk-tprkb and uses thereof |
WO2014023081A1 (en) * | 2012-08-07 | 2014-02-13 | 中国科学院上海生命科学研究院 | Artemisinin derivatives, preparation process and use thereof |
US20160058872A1 (en) * | 2014-04-14 | 2016-03-03 | Arvinas, Inc. | Imide-based modulators of proteolysis and associated methods of use |
Non-Patent Citations (3)
Title |
---|
JARMAN, M. ET AL.: "Selective inhibition of cholesterol side-chain cleavage by potential pro-drug forms of aminoglutethimide", ANTI-CANCER DRUG DESIGN, vol. 3, 1988, pages 185 - 190, XP009517051 * |
JONATHAN W. GRANT ET AL: "Toward the Development of a Cephalosporin-Based Dual-Release Prodrug for Use in ADEPT", JOURNAL OF ORGANIC CHEMISTRY, vol. 69, no. 23, 1 November 2004 (2004-11-01), US, pages 7965 - 7970, XP055639681, ISSN: 0022-3263, DOI: 10.1021/jo048970i * |
See also references of WO2017197046A1 * |
Also Published As
Publication number | Publication date |
---|---|
EP3455218A1 (en) | 2019-03-20 |
US11992531B2 (en) | 2024-05-28 |
US20220313826A1 (en) | 2022-10-06 |
US20190076542A1 (en) | 2019-03-14 |
CN109641874A (en) | 2019-04-16 |
US10849982B2 (en) | 2020-12-01 |
WO2017197046A1 (en) | 2017-11-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP3455218A4 (en) | C3-carbon linked glutarimide degronimers for target protein degradation | |
EP3454856A4 (en) | Heterocyclic degronimers for target protein degradation | |
EP3455219A4 (en) | Amine-linked c3-glutarimide degronimers for target protein degradation | |
EP3454862A4 (en) | Spirocyclic degronimers for target protein degradation | |
EP3652329A4 (en) | Compounds for tau protein degradation | |
EP3450452A4 (en) | Modified fibroin | |
EP3450451A4 (en) | Modified fibroin | |
EP3197453B8 (en) | Chimeric protein | |
EP3347035A4 (en) | Cartilage-homing peptides | |
EP3578570A4 (en) | Multifunctional protein | |
EP3476859A4 (en) | Modified fibroin | |
EP3349582A4 (en) | Novel insect inhibitory proteins | |
EP3369741A4 (en) | Novel peptide | |
EP3467106A4 (en) | Peptide compound | |
EP3496662A4 (en) | Silk-derived protein for treating inflammation | |
EP3562299A4 (en) | Insecticidal proteins | |
EP3385266A4 (en) | Compound for specific binding with amyloid protein | |
EP3288931A4 (en) | Certain protein kinase inhibitor | |
EP3526251A4 (en) | Anti-p53 antibodies | |
EP3531824A4 (en) | Insecticidal proteins | |
EP3563840A4 (en) | Patch | |
EP3309163A4 (en) | Substituted dihydropyrrolopyrazole derivative | |
EP3312278A4 (en) | Protein expression method | |
EP3347712A4 (en) | Methods of identifying drug-modulated polypeptide targets for degradation | |
EP3463414A4 (en) | Protein interfaces |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE |
|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
17P | Request for examination filed |
Effective date: 20181206 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
AX | Request for extension of the european patent |
Extension state: BA ME |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: HE, MINSHENG Inventor name: NASVESCHUK, CHRIS, G. Inventor name: LIANG, YANKE Inventor name: PHILLIPS, ANDREW, J. Inventor name: LAZARSKI, KIEL Inventor name: HENDERSON, JAMES, A. Inventor name: VEITS, GESINE, KERSTIN Inventor name: VORA, HARIT, U. |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: LIANG, YANKE Inventor name: VEITS, GESINE, KERSTIN Inventor name: HE, MINSHENG Inventor name: PHILLIPS, ANDREW, J. Inventor name: NASVESCHUK, CHRIS, G. Inventor name: VORA, HARIT, U. Inventor name: LAZARSKI, KIEL Inventor name: HENDERSON, JAMES, A. |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: HE, MINSHENG Inventor name: PHILLIPS, ANDREW, J. Inventor name: LAZARSKI, KIEL Inventor name: VEITS, GESINE, KERSTIN Inventor name: VORA, HARIT, U. Inventor name: LIANG, YANKE Inventor name: NASVESCHUK, CHRIS, G. Inventor name: HENDERSON, JAMES, A. |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: LIANG, YANKE Inventor name: PHILLIPS, ANDREW, J. Inventor name: HE, MINSHENG Inventor name: NASVESCHUK, CHRIS, G. Inventor name: VEITS, GESINE, KERSTIN Inventor name: VORA, HARIT, U. Inventor name: HENDERSON, JAMES, A. Inventor name: LAZARSKI, KIEL |
|
DAV | Request for validation of the european patent (deleted) | ||
DAX | Request for extension of the european patent (deleted) | ||
A4 | Supplementary search report drawn up and despatched |
Effective date: 20191118 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: C07D 401/14 20060101AFI20191112BHEP Ipc: C07K 14/72 20060101ALI20191112BHEP Ipc: C07K 14/47 20060101ALI20191112BHEP |
|
REG | Reference to a national code |
Ref country code: HK Ref legal event code: DE Ref document number: 40004898 Country of ref document: HK |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
17Q | First examination report despatched |
Effective date: 20201126 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
P01 | Opt-out of the competence of the unified patent court (upc) registered |
Effective date: 20230528 |
|
TPAC | Observations filed by third parties |
Free format text: ORIGINAL CODE: EPIDOSNTIPA |
|
TPAC | Observations filed by third parties |
Free format text: ORIGINAL CODE: EPIDOSNTIPA |